Centre for Neuroscience and Trauma, The Blizard Institute of Cell and Molecular Science, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
J Neurotrauma. 2010 Oct;27(10):1769-80. doi: 10.1089/neu.2010.1348. Epub 2010 Oct 6.
We have previously shown that the omega-3 fatty acid docosahexaenoic acid (DHA) significantly improves several histological and behavioral measures after spinal cord injury (SCI). White matter damage plays a key role in neurological outcome following SCI. Therefore, we examined the effects of the acute intravenous (IV) administration of DHA (250 nmol/kg) 30 min after thoracic compression SCI in rats, alone or in combination with a DHA-enriched diet (400 mg/kg/d, administered for 6 weeks post-injury), on white matter pathology. By 1 week post-injury, the acute IV DHA injection led to significantly reduced axonal dysfunction, as indicated by accumulation of β-amyloid precursor protein (-55% compared to vehicle-injected controls) in the dorsal columns. The loss of cytoskeletal proteins following SCI was also significantly reduced. There were 43% and 73% more axons immunoreactive for non-phosphorylated 200-kD neurofilament in the ventral white matter and ventrolateral white matter, respectively, in animals receiving DHA injections than vehicle-injected rats. The acute DHA treatment also led to a significant improvement in microtubule-associated protein-2 immunoreactivity. By 6 weeks, damage to myelin and serotonergic fibers was also reduced. For some of the parameters measured, the combination of DHA injection and DHA-enriched diet led to greater neuroprotection than DHA injection alone. These findings demonstrate the therapeutic potential of DHA in SCI, and clearly indicate that this fatty acid confers significant protection to the white matter.
我们之前已经表明,ω-3 脂肪酸二十二碳六烯酸(DHA)可显著改善脊髓损伤(SCI)后的几种组织学和行为测量。 白质损伤在 SCI 后的神经功能结果中起着关键作用。 因此,我们检查了在大鼠胸压缩 SCI 后 30 分钟急性静脉内(IV)给予 DHA(250 nmol/kg)(单独或与富含 DHA 的饮食(400 mg/kg/d,在损伤后 6 周给予)联合使用)对白质病理学的影响。 在损伤后 1 周,急性 IV DHA 注射导致轴突功能障碍明显减少,这表明背柱中β-淀粉样前体蛋白(与载体注射对照相比减少了 55%)积聚。 SCI 后细胞骨架蛋白的丢失也明显减少。 在接受 DHA 注射的动物中,腹侧白质和腹外侧白质中分别有 43%和 73%更多的非磷酸化 200-kD 神经丝免疫反应性轴突,而非载体注射大鼠。 急性 DHA 处理还导致微管相关蛋白-2 免疫反应性显著改善。 到 6 周时,髓鞘和 5-羟色胺能纤维的损伤也减少了。 对于所测量的一些参数,DHA 注射和富含 DHA 的饮食联合使用比 DHA 注射本身具有更大的神经保护作用。 这些发现表明 DHA 在 SCI 中的治疗潜力,并清楚地表明这种脂肪酸对白质具有重要的保护作用。